We report on the synthesis of Y nanoclusters and a particular chemical soli
d-state reaction of these clusters YH2 double left right arrow YH3, which h
as recently received increasing interest in the case of continuous thin fil
ms, We used a novel type of laser ablation cluster source to synthesize Y-c
lusters of about 25-30 nm average size at different Ar background gas press
ures to hydrogenize them in situ. The clusters were characterized by electr
on microscopy and optical spectroscopy. It was found that clusters prepared
in higher Ar gas pressure consist of Y-core and Y2O3-shell contrary to Y-c
lusters synthesized at low Ar gas conditions. Analysis of corresponding ext
inction spectra were made by Mie theory calculations. Reaction with hydroge
n was observed only for deposited Y-clusters which were hydrogenated at roo
m temperature by adding atomic H. In a first step the metallic dihydride (Y
H2) is formed. In a second step, additional H can form YH3-x (x < 1 to x mu
ch less than 1). The latter compound is electrically isolating. The fascina
ting properties of the last reaction are its reversibility at room temperat
ure and the combination of a structural phase transition and a metal/non-me
tal transition. The reversible phase transition was monitored by the optica
l spectra which exhibit several strong and selective Mie resonances. (C) 20
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